Journal of inflammation research · 2025
ZnO NPs Attenuate LPS-Induced Inflammation in RAW264.7 Macrophages by Inhibiting NF-κB and JAK1-STAT1/STAT3 Pathways and Reducing ROS.
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Tang Hui, Zhang Li, Deng Chengchen, Li Yuechuan, Ren Guiying, Sun Ziru, Chang Lebing, Xu Meihong, Xiao Duanqiang, Zhang Haijun
Аннотация
BACKGROUND: Macrophage-mediated inflammatory signaling drives pathological inflammation in diverse diseases. Zinc oxide nanoparticles (ZnO NPs) exhibit recognized anti-inflammatory activity, but their precise molecular mechanisms remain unclear. This study investigates the modulatory effects of ZnO NPs on Lipopolysaccharide (LPS)-induced inflammatory and underlying pathways in RAW264.7 macrophages.
METHODS: Scanning electron microscopy (SEM) was used to analyze the primary particle sizes of ZnO NPs. Their cytotoxicity on RAW264.7 cells was assessed using the CCK-8 assay. Cells were pretreated with ZnO NPs (0, 0.5, 1, 2, 5 μg/mL) for 1 h, then stimulated with LPS (1 μg/mL) for 24 h. Pro-inflammatory factors (TNF-α, IL-1β, IL-6, iNOS, and COX-2), as well as the anti-inflammatory factor Arg-1, were detected using qRT-PCR, ELISA, or Western blot. RNA-sequencing identified differentially expressed genes (DEGs). Nitric oxide (NO) production, Reactive Oxygen Species (ROS).
RESULTS: ZnO NPs reduced LPS-induced production of NO and pro-inflammatory factors but increased Arg-1 expression. RNA-sequencing identified 2638 DEGs (1822 upregulated, 816 downregulated) between LPS and LPS+ZnO NPs groups. Mechanistically, ZnO NPs exerted anti-inflammatory effects through: (1) blocking NF-κB activation by inhibiting IκB-α degradation and p65 nuclear translocation; (2) suppressing JAK1-mediated STAT1/3 activation and nuclear translocation. They also reduced LPS-induced ROS.
CONCLUSION: ZnO NPs mitigate LPS-triggered inflammation by targeting NF-κB and JAK1-STAT1/3 pathways, and reducing ROS. These findings provide novel mechanistic insights into the anti-inflammatory effects of ZnO NPs, highlighting their therapeutic potential in macrophage-associated inflammatory disorders.
METHODS: Scanning electron microscopy (SEM) was used to analyze the primary particle sizes of ZnO NPs. Their cytotoxicity on RAW264.7 cells was assessed using the CCK-8 assay. Cells were pretreated with ZnO NPs (0, 0.5, 1, 2, 5 μg/mL) for 1 h, then stimulated with LPS (1 μg/mL) for 24 h. Pro-inflammatory factors (TNF-α, IL-1β, IL-6, iNOS, and COX-2), as well as the anti-inflammatory factor Arg-1, were detected using qRT-PCR, ELISA, or Western blot. RNA-sequencing identified differentially expressed genes (DEGs). Nitric oxide (NO) production, Reactive Oxygen Species (ROS).
RESULTS: ZnO NPs reduced LPS-induced production of NO and pro-inflammatory factors but increased Arg-1 expression. RNA-sequencing identified 2638 DEGs (1822 upregulated, 816 downregulated) between LPS and LPS+ZnO NPs groups. Mechanistically, ZnO NPs exerted anti-inflammatory effects through: (1) blocking NF-κB activation by inhibiting IκB-α degradation and p65 nuclear translocation; (2) suppressing JAK1-mediated STAT1/3 activation and nuclear translocation. They also reduced LPS-induced ROS.
CONCLUSION: ZnO NPs mitigate LPS-triggered inflammation by targeting NF-κB and JAK1-STAT1/3 pathways, and reducing ROS. These findings provide novel mechanistic insights into the anti-inflammatory effects of ZnO NPs, highlighting their therapeutic potential in macrophage-associated inflammatory disorders.